TW501925B - Preventive-therapeutic drug for Alzheimer's disease - Google Patents

Preventive-therapeutic drug for Alzheimer's disease Download PDF

Info

Publication number: TW501925B
Authority: TW; Taiwan
Prior art keywords: alzheimer; disease; cells; preventive; phenyl
Prior art date: 1996-08-27

Application number

TW086112018A

Other languages

English (en)

Chinese (zh)

Inventor

Hiroyuki Masayasu

Ikuro Maruyama

Kazuhiro Abeyama

Original Assignee

Daiichi Seiyaku Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-08-27

Filing date

1997-08-21

Publication date

2002-09-11

1997-08-21 Application filed by Daiichi Seiyaku Co filed Critical Daiichi Seiyaku Co

2002-09-11 Application granted granted Critical

2002-09-11 Publication of TW501925B publication Critical patent/TW501925B/zh

Links

208000024827 Alzheimer disease Diseases 0.000 title abstract description 15
229940126585 therapeutic drug Drugs 0.000 title abstract description 3
150000003839 salts Chemical class 0.000 claims abstract description 15
239000003814 drug Substances 0.000 claims abstract description 10
239000004480 active ingredient Substances 0.000 claims abstract description 6
102000013455 Amyloid beta-Peptides Human genes 0.000 claims abstract description 5
108010090849 Amyloid beta-Peptides Proteins 0.000 claims abstract description 5
230000003449 preventive effect Effects 0.000 claims abstract description 5
150000002576 ketones Chemical class 0.000 claims description 5
230000016273 neuron death Effects 0.000 claims description 5
229940124597 therapeutic agent Drugs 0.000 claims description 5
201000010099 disease Diseases 0.000 claims description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 2
229940121649 protein inhibitor Drugs 0.000 claims 1
239000012268 protein inhibitor Substances 0.000 claims 1
DYEFUKCXAQOFHX-UHFFFAOYSA-N Ebselen Chemical compound [se]1C2=CC=CC=C2C(=O)N1C1=CC=CC=C1 DYEFUKCXAQOFHX-UHFFFAOYSA-N 0.000 abstract description 13
210000002569 neuron Anatomy 0.000 abstract description 6
230000034994 death Effects 0.000 abstract description 5
229940079593 drug Drugs 0.000 abstract description 5
230000002265 prevention Effects 0.000 abstract description 5
210000004027 cell Anatomy 0.000 description 24
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 14
229950010033 ebselen Drugs 0.000 description 12
230000000694 effects Effects 0.000 description 7
108010039918 Polylysine Proteins 0.000 description 6
230000002401 inhibitory effect Effects 0.000 description 6
229920000656 polylysine Polymers 0.000 description 6
239000006144 Dulbecco’s modiﬁed Eagle's medium Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
241000700159 Rattus Species 0.000 description 4
230000002079 cooperative effect Effects 0.000 description 4
239000003112 inhibitor Substances 0.000 description 4
239000002609 medium Substances 0.000 description 4
210000002966 serum Anatomy 0.000 description 4
238000012360 testing method Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
230000004888 barrier function Effects 0.000 description 3
-1 benzo Isoselenazol-3 (2H) -one Chemical compound 0.000 description 3
230000030833 cell death Effects 0.000 description 3
239000006285 cell suspension Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000003937 drug carrier Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000011669 selenium Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
208000037259 Amyloid Plaque Diseases 0.000 description 2
206010029350 Neurotoxicity Diseases 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
206010044221 Toxic encephalopathy Diseases 0.000 description 2
239000002775 capsule Substances 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
230000000875 corresponding effect Effects 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
239000008298 dragée Substances 0.000 description 2
238000001943 fluorescence-activated cell sorting Methods 0.000 description 2
238000001727 in vivo Methods 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
239000002207 metabolite Substances 0.000 description 2
239000000203 mixture Substances 0.000 description 2
231100000228 neurotoxicity Toxicity 0.000 description 2
230000007135 neurotoxicity Effects 0.000 description 2
229910052711 selenium Inorganic materials 0.000 description 2
239000000243 solution Substances 0.000 description 2
230000004083 survival effect Effects 0.000 description 2
239000000725 suspension Substances 0.000 description 2
210000004881 tumor cell Anatomy 0.000 description 2
CZICLKKAVOBWSW-UHFFFAOYSA-N 1,2-selenazole Chemical compound C=1C=N[se]C=1 CZICLKKAVOBWSW-UHFFFAOYSA-N 0.000 description 1
XDFNWJDGWJVGGN-UHFFFAOYSA-N 2-(2,7-dichloro-3,6-dihydroxy-9h-xanthen-9-yl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C1C2=CC(Cl)=C(O)C=C2OC2=CC(O)=C(Cl)C=C21 XDFNWJDGWJVGGN-UHFFFAOYSA-N 0.000 description 1
FIISKTXZUZBTRC-UHFFFAOYSA-N 2-phenyl-1,3-benzoxazole Chemical compound C1=CC=CC=C1C1=NC2=CC=CC=C2O1 FIISKTXZUZBTRC-UHFFFAOYSA-N 0.000 description 1
SYWIVWYYBHYXCI-UHFFFAOYSA-N 2-phenyl-3h-1,2-benzoselenazole Chemical compound [Se]1C2=CC=CC=C2CN1C1=CC=CC=C1 SYWIVWYYBHYXCI-UHFFFAOYSA-N 0.000 description 1
MHVNUMRNTNTZJH-UHFFFAOYSA-N 2-phenyl-9h-fluorene Chemical compound C1=C2CC3=CC=CC=C3C2=CC=C1C1=CC=CC=C1 MHVNUMRNTNTZJH-UHFFFAOYSA-N 0.000 description 1
102000012440 Acetylcholinesterase Human genes 0.000 description 1
108010022752 Acetylcholinesterase Proteins 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
241000283086 Equidae Species 0.000 description 1
241000406668 Loxodonta cyclotis Species 0.000 description 1
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
239000004472 Lysine Substances 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
241000699666 Mus <mouse, genus> Species 0.000 description 1
241000699670 Mus sp. Species 0.000 description 1
206010067482 No adverse event Diseases 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
102000004142 Trypsin Human genes 0.000 description 1
108090000631 Trypsin Proteins 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
229940022698 acetylcholinesterase Drugs 0.000 description 1
230000004520 agglutination Effects 0.000 description 1
230000001270 agonistic effect Effects 0.000 description 1
125000000539 amino acid group Chemical group 0.000 description 1
238000003782 apoptosis assay Methods 0.000 description 1
XKRFYHLGVUSROY-UHFFFAOYSA-N argon Substances [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000002981 blocking agent Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
239000011651 chromium Substances 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000007887 coronary angioplasty Methods 0.000 description 1
238000012937 correction Methods 0.000 description 1
210000004748 cultured cell Anatomy 0.000 description 1
230000006806 disease prevention Effects 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000010255 intramuscular injection Methods 0.000 description 1
239000007927 intramuscular injection Substances 0.000 description 1
238000007912 intraperitoneal administration Methods 0.000 description 1
238000001990 intravenous administration Methods 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
239000002502 liposome Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
DKXULEFCEORBJK-UHFFFAOYSA-N magnesium;octadecanoic acid Chemical compound [Mg].CCCCCCCCCCCCCCCCCC(O)=O DKXULEFCEORBJK-UHFFFAOYSA-N 0.000 description 1
238000000034 method Methods 0.000 description 1
239000003068 molecular probe Substances 0.000 description 1
230000000926 neurological effect Effects 0.000 description 1
231100000189 neurotoxic Toxicity 0.000 description 1
230000002887 neurotoxic effect Effects 0.000 description 1
239000003883 ointment base Substances 0.000 description 1
230000001575 pathological effect Effects 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
239000006187 pill Substances 0.000 description 1
239000002574 poison Substances 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
239000000843 powder Substances 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
230000005522 programmed cell death Effects 0.000 description 1
230000000069 prophylactic effect Effects 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
208000037803 restenosis Diseases 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000010802 sludge Substances 0.000 description 1
239000007901 soft capsule Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
238000010254 subcutaneous injection Methods 0.000 description 1
239000007929 subcutaneous injection Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
239000012588 trypsin Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

Landscapes

Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Biomedical Technology (AREA)
Bioinformatics & Cheminformatics (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Hospice & Palliative Care (AREA)
Psychiatry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Medicinal Preparation (AREA)

TW086112018A 1996-08-27 1997-08-21 Preventive-therapeutic drug for Alzheimer's disease TW501925B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP22551296		1996-08-27

Publications (1)

Publication Number	Publication Date
TW501925B true TW501925B (en)	2002-09-11

Family

ID=16830487

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW086112018A TW501925B (en)	1996-08-27	1997-08-21	Preventive-therapeutic drug for Alzheimer's disease

Country Status (28)

Country	Link
US (1)	US5948800A (lt)
EP (1)	EP0826370B1 (lt)
KR (1)	KR20000035859A (lt)
CN (1)	CN1112922C (lt)
AT (1)	ATE219361T1 (lt)
AU (2)	AU3866997A (lt)
BR (1)	BR9711259A (lt)
CA (1)	CA2213794C (lt)
CZ (1)	CZ295364B6 (lt)
DE (2)	DE59707550D1 (lt)
DK (1)	DK0826370T3 (lt)
EE (1)	EE03953B1 (lt)
ES (1)	ES2177849T3 (lt)
FI (1)	FI119622B (lt)
HU (1)	HU225264B1 (lt)
IL (1)	IL127113A (lt)
LT (1)	LT4602B (lt)
LV (1)	LV12251B (lt)
NO (1)	NO312812B1 (lt)
NZ (1)	NZ332292A (lt)
PL (1)	PL188481B1 (lt)
PT (1)	PT826370E (lt)
SI (1)	SI9720060B (lt)
TR (1)	TR199700858A2 (lt)
TW (1)	TW501925B (lt)
UA (1)	UA59367C2 (lt)
WO (2)	WO1998008511A1 (lt)
ZA (1)	ZA977644B (lt)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES2145065T3 (es) *	1993-10-27	2000-07-01	Daiichi Seiyaku Co	Preparacion granular.
JP2000016935A (ja) *	1998-07-01	2000-01-18	Dai Ichi Seiyaku Co Ltd	シクロオキシゲナーゼ阻害剤
AU3457300A (en)	1999-03-31	2000-10-16	Daiichi Pharmaceutical Co., Ltd.	Substrates for thioredoxin reductase
WO2003010143A1 (en)	2001-07-26	2003-02-06	Samsung Electronics Co., Ltd.	Dialkylhydroxybenzoic acid derivatives containing metal chelating groups and their therapeutic uses
WO2003010154A1 (en) *	2001-07-26	2003-02-06	Samsung Electronics Co. Ltd.	Seleno compounds containing nitrone moiety, their preparation and their therapeutic uses
WO2003010153A1 (en)	2001-07-26	2003-02-06	Samsung Electronics Co. Ltd.	N-alkyl-n-phenylhydroxylamine compounds containing metal chelating groups, their preparation and their therapeutic uses
GB201102248D0 (en)	2011-02-09	2011-03-23	Isis Innovation	Treatment of bipolar disorder
CN103965188A (zh) *	2013-01-29	2014-08-06	中山大学	含硒多奈哌齐类似物
EP2950102A1 (en)	2014-05-30	2015-12-02	Biocross, S.L.	Method for the diagnosis of alzheimer s disease and mild cognitive impairment
US10058542B1 (en)	2014-09-12	2018-08-28	Thioredoxin Systems Ab	Composition comprising selenazol or thiazolone derivatives and silver and method of treatment therewith
EP3067699A1 (en)	2015-03-11	2016-09-14	Neuron Bio, S.A.	Method for diagnosing alzheimer's disease
PL237739B1 (pl)	2018-06-06	2021-05-17	Univ Gdanski	Genisteina do zastosowania do leczenia choroby Alzheimera
CN113116888B (zh) *	2021-04-19	2022-08-26	上海兴糖生物技术有限公司	依布硒啉的用途

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3616923A1 (de) *	1986-05-20	1987-11-26	Nattermann A & Cie	Neue pharmazeutische verwendung von 2-phenyl-1,2-benzisoselenazol-3(2h)-on
DE3638124C2 (de) *	1986-11-08	1996-09-05	Nattermann A & Cie	Neue pharmazeutische Verwendung von Ebselen
JPH01131113A (ja) *	1987-08-27	1989-05-24	Dai Ichi Seiyaku Co Ltd	脳障害治療剤
JPH0238591A (ja)	1988-07-27	1990-02-07	Fujikura Ltd	高純度銅の製造方法
DE4024885C2 (de) *	1990-08-06	2002-07-18	Nattermann A & Cie	Verwendung von 2-Phenyl-1,2-benzisoselenazol-3(2H)-on
US5385726A (en) *	1990-08-06	1995-01-31	Rhone-Poulenc Rorer Gmbh	Use of 2-phenyl-1,2-benzisoselenazol-3-(2H)-one
FR2669633B1 (fr) *	1990-11-23	1993-01-22	Adir	Nouveaux derives de la benzoselenazolinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
JPH07233056A (ja) *	1993-09-03	1995-09-05	Dai Ichi Seiyaku Co Ltd	リポキシゲナーゼ阻害剤

1997
- 1997-03-17 ES ES97104503T patent/ES2177849T3/es not_active Expired - Lifetime
- 1997-03-17 DE DE59707550T patent/DE59707550D1/de not_active Expired - Fee Related
- 1997-03-17 PT PT97104503T patent/PT826370E/pt unknown
- 1997-03-17 DK DK97104503T patent/DK0826370T3/da active
- 1997-03-17 AT AT97104503T patent/ATE219361T1/de not_active IP Right Cessation
- 1997-03-17 EP EP97104503A patent/EP0826370B1/de not_active Expired - Lifetime
- 1997-04-07 SI SI9720060A patent/SI9720060B/sl not_active IP Right Cessation
- 1997-04-07 BR BR9711259A patent/BR9711259A/pt not_active Application Discontinuation
- 1997-04-07 IL IL12711397A patent/IL127113A/xx not_active IP Right Cessation
- 1997-04-07 WO PCT/DE1997/000701 patent/WO1998008511A1/de not_active Ceased
- 1997-04-07 EE EEP199900007A patent/EE03953B1/xx not_active IP Right Cessation
- 1997-04-07 HU HU9903213A patent/HU225264B1/hu not_active IP Right Cessation
- 1997-04-07 CZ CZ1999317A patent/CZ295364B6/cs not_active IP Right Cessation
- 1997-04-07 NZ NZ332292A patent/NZ332292A/en unknown
- 1997-04-07 CN CN97195890A patent/CN1112922C/zh not_active Expired - Fee Related
- 1997-07-04 UA UA99010526A patent/UA59367C2/uk unknown
- 1997-08-04 US US08/905,530 patent/US5948800A/en not_active Expired - Lifetime
- 1997-08-04 DE DE19733690A patent/DE19733690A1/de not_active Withdrawn
- 1997-08-20 WO PCT/JP1997/002883 patent/WO1998008831A1/ja not_active Ceased
- 1997-08-20 AU AU38669/97A patent/AU3866997A/en not_active Abandoned
- 1997-08-20 KR KR1019997001554A patent/KR20000035859A/ko not_active Ceased
- 1997-08-21 TW TW086112018A patent/TW501925B/zh not_active IP Right Cessation
- 1997-08-25 CA CA002213794A patent/CA2213794C/en not_active Expired - Fee Related
- 1997-08-26 PL PL97321796A patent/PL188481B1/pl not_active IP Right Cessation
- 1997-08-26 AU AU35298/97A patent/AU725534B2/en not_active Ceased
- 1997-08-26 ZA ZA977644A patent/ZA977644B/xx unknown
- 1997-08-26 NO NO19973912A patent/NO312812B1/no not_active IP Right Cessation
- 1997-08-27 TR TR97/00858A patent/TR199700858A2/xx unknown
1998
- 1998-10-22 LV LVP-98-231A patent/LV12251B/lv unknown
- 1998-12-11 FI FI982689A patent/FI119622B/fi not_active IP Right Cessation
1999
- 1999-02-23 LT LT99-016A patent/LT4602B/lt not_active IP Right Cessation

Also Published As

Publication number	Publication date
HU225264B1 (en)	2006-08-28
UA59367C2 (uk)	2003-09-15
NO973912D0 (no)	1997-08-26
AU3866997A (en)	1998-03-19
IL127113A (en)	2003-07-06
CN1223580A (zh)	1999-07-21
WO1998008511A1 (de)	1998-03-05
TR199700858A2 (xx)	1998-03-21
PL188481B1 (pl)	2005-02-28
NO973912L (no)	1998-03-02
CA2213794C (en)	2006-10-03
LV12251B (lv)	1999-08-20
PL321796A1 (en)	1998-03-02
SI9720060B (en)	2001-12-31
BR9711259A (pt)	1999-08-17
FI119622B (fi)	2009-01-30
EE9900007A (et)	1999-06-15
NZ332292A (en)	2001-07-27
EE03953B1 (et)	2003-02-17
DE19733690A1 (de)	1998-03-26
DK0826370T3 (da)	2002-10-07
CA2213794A1 (en)	1998-02-27
CZ295364B6 (cs)	2005-07-13
FI982689L (fi)	1998-12-11
LV12251A (lv)	1999-04-20
ATE219361T1 (de)	2002-07-15
US5948800A (en)	1999-09-07
EP0826370B1 (de)	2002-06-19
KR20000035859A (ko)	2000-06-26
DE59707550D1 (de)	2002-07-25
FI982689A0 (fi)	1998-12-11
ZA977644B (en)	1999-02-26
HK1020317A1 (en)	2000-04-14
LT4602B (lt)	2000-01-25
HUP9903213A1 (en)	2000-07-28
CZ31799A3 (cs)	1999-11-17
HUP9903213A3 (en)	2000-12-28
SI9720060A (sl)	1999-06-30
AU725534B2 (en)	2000-10-12
NO312812B1 (no)	2002-07-08
AU3529897A (en)	1998-03-05
CN1112922C (zh)	2003-07-02
LT99016A (lt)	1999-10-25
ES2177849T3 (es)	2002-12-16
EP0826370A1 (de)	1998-03-04
IL127113A0 (en)	1999-09-22
WO1998008831A1 (en)	1998-03-05
PT826370E (pt)	2002-10-31

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2005-12-01	MM4A	Annulment or lapse of patent due to non-payment of fees

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